1ZT4
The crystal structure of human CD1d with and without alpha-Galactosylceramide
Summary for 1ZT4
Entry DOI | 10.2210/pdb1zt4/pdb |
Descriptor | T-cell surface glycoprotein CD1d, Beta-2-microglobulin, N-{(1S,2R,3S)-1-[(ALPHA-D-GALACTOPYRANOSYLOXY)METHYL]-2,3-DIHYDROXYHEPTADECYL}HEXACOSANAMIDE, ... (4 entities in total) |
Functional Keywords | human cd1d, cd1, mhc class i, empty binding groove, glycolipid, alpha-galactosylceramide, alpha-galcer, structural proteomics in europe, spine, structural genomics, immune system |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 4 |
Total formula weight | 88254.66 |
Authors | Koch, M.,Stronge, V.S.,Shepherd, D.,Gadola, S.D.,Mathew, B.,Ritter, G.,Fersht, A.R.,Besra, G.S.,Schmidt, R.R.,Jones, E.Y.,Cerundolo, V.,Structural Proteomics in Europe (SPINE) (deposition date: 2005-05-26, release date: 2005-07-19, Last modification date: 2024-11-20) |
Primary citation | Koch, M.,Stronge, V.S.,Shepherd, D.,Gadola, S.D.,Mathew, B.,Ritter, G.,Fersht, A.R.,Besra, G.S.,Schmidt, R.R.,Jones, E.Y.,Cerundolo, V. The crystal structure of human CD1d with and without alpha-galactosylceramide Nat.Immunol., 6:819-826, 2005 Cited by PubMed Abstract: The glycolipid alpha-galactosylceramide binds with high affinity to CD1d and stimulates natural killer T cells. Here we report the crystal structure of human CD1d in complex with synthetic alpha-galactosylceramide at a resolution of 3.0 A. The structure shows a tightly fit lipid in the CD1d binding groove, with the sphingosine chain bound in the C' pocket and the longer acyl chain anchored in the A' pocket. We also present the CD1d structure without lipid, which has a more open conformation of the binding groove, suggesting a dual conformation of CD1d in which the 'open' conformation is more able to load lipids. These structures provide clues as to how CD1 molecules load glycolipids as well as data to guide the design of new therapeutic agents. PubMed: 16007090DOI: 10.1038/ni1225 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3 Å) |
Structure validation
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